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myopic CNV update- 4 months on…
Morning, just to update people who might be less far along than I am incase you are interested. Also just to be clear my experiences are limited and based on myopic CNV not wet AMD or dry AMD. So back in April I had a CNV in my left eye, treated 3 weeks later by Eylea x 2- one in May, one in June. It
Morning, just to update people who might be less far along than I am incase you are interested. Also just to be clear my experiences are limited and based on myopic CNV not wet AMD or dry AMD. So back in April I had a CNV in my left eye, treated 3 weeks later by Eylea x 2- one in May, one in June. It
Deepbluesea2022
in
Macular Society
2 years ago
Need advice
Had Hashimotos since 2008. Never felt well so after all these years, decided to try Tiromel to see if it makes a difference. Started off with quarter of a tab (1 week) then half a tab (2 weeks) & today started on a full one. Too early to tell if will make a difference. Also started SI vit b12 EOD with
Had Hashimotos since 2008. Never felt well so after all these years, decided to try Tiromel to see if it makes a difference. Started off with quarter of a tab (1 week) then half a tab (2 weeks) & today started on a full one. Too early to tell if will make a difference. Also started SI vit b12 EOD with
Cerezo
in
Thyroid UK
2 years ago
Warm and hot uncomfortable body with Statins or?
I am on daily crestor 10mg,1 ezetrol, 2 berlinda tablets and 1 esprin for year and half after having 4 stents and recently from last 3 months I am feeling that my body stays warm and I feel hot not sweaty but uncomfortable hot. anyone have similar experience. any tips or help?
I am on daily crestor 10mg,1 ezetrol, 2 berlinda tablets and 1 esprin for year and half after having 4 stents and recently from last 3 months I am feeling that my body stays warm and I feel hot not sweaty but uncomfortable hot. anyone have similar experience. any tips or help?
1975A
in
British Heart Foundation
2 years ago
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Please help! At a loss with my dad's symptoms and GP
Hi all, Just joined this as not sure where else to turn! My Dad is 72 and in November 2020 his bloods showed that he was low in b12 (sorry don't have exact result). At the time I was baffled by this as he was eating eggs daily and ate red meat regularly too. After a quick search I read about PA and
Hi all, Just joined this as not sure where else to turn! My Dad is 72 and in November 2020 his bloods showed that he was low in b12 (sorry don't have exact result). At the time I was baffled by this as he was eating eggs daily and ate red meat regularly too. After a quick search I read about PA and
Needleandthread44
in
Pernicious Anaemia Society
2 years ago
7th week post partial circumcision - Experience so far !!
To encounter this, I recently ordered a
castor
oil
and going to apply and getting used to it from next week onwards. But I always have plan B if I am going out or for any sort of outdoor activities I mentioned I always pull back the foreskin on top of my glans to avoid any discomfort.
To encounter this, I recently ordered a
castor
oil
and going to apply and getting used to it from next week onwards. But I always have plan B if I am going out or for any sort of outdoor activities I mentioned I always pull back the foreskin on top of my glans to avoid any discomfort.
phantomblack
in
Men's Health Forum (Penis Health)
3 years ago
Can’t sleep
I dunno why I can’t sleep ; took dopamine (I have YOPD), dopamine agonist to take care of RLS, magnesium to calm me down, warm shower , massaged my feet with lukewarm mustard oil, rubbed peppermint oil on pillow, put cucumbers on eyes but still can’t.. been three hours!
I dunno why I can’t sleep ; took dopamine (I have YOPD), dopamine agonist to take care of RLS, magnesium to calm me down, warm shower , massaged my feet with lukewarm mustard oil, rubbed peppermint oil on pillow, put cucumbers on eyes but still can’t.. been three hours!
Divii
in
Sleep Matters
2 years ago
Struggling with a diagnosis
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Ryane96
in
Fibromyalgia Action UK
2 years ago
Struggling for a diagnosis
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease ,apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Hello, I have been suffering with what I believe are all symptoms of an unknown autoimmune disease ,apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme
Ryane96
in
NRAS
2 years ago
Struggling to get a diagnosis.
Hello, I have been suffering with what I believe are all symptoms of lupus, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme debilitating fatigue
Hello, I have been suffering with what I believe are all symptoms of lupus, apart from a face rash and organ damage, for around 4 years. My blood results showed positive for HLAB27 & ANA ELISA with a low titre rheumatoid factor. I also suffer with psoriasis, hair loss, extreme debilitating fatigue
Ryane96
in
LUPUS UK
2 years ago
New PMR Sufferer
Hi, as a new PMR sufferer, I am keen to hear from similar sufferers of the condition! I consider my symptoms as moderate and I appear to be managing my condition reasonably well with 15mg of Prednisolone. I also supplement my diet with Magnesium and Vitamin D, a daily dose of Cod Liver oil. I actively
Hi, as a new PMR sufferer, I am keen to hear from similar sufferers of the condition! I consider my symptoms as moderate and I appear to be managing my condition reasonably well with 15mg of Prednisolone. I also supplement my diet with Magnesium and Vitamin D, a daily dose of Cod Liver oil. I actively
LTDWJ
in
PMRGCAuk
2 years ago
Supplements
Hi Everyone , Had a few suggestions of supplements I could take which will help me dealing with my arthritis. These were Cod liver oil capsules- great for taking care of your joints Glucosamine and Condroitin - also great for taking care of your joints . Finally Coenzyme Q10 which improves your energy
Hi Everyone , Had a few suggestions of supplements I could take which will help me dealing with my arthritis. These were Cod liver oil capsules- great for taking care of your joints Glucosamine and Condroitin - also great for taking care of your joints . Finally Coenzyme Q10 which improves your energy
Bluegolf1975
in
NRAS
2 years ago
I have my 5th shot today🤞🏻
Hey everyone. I have my 5th shot due today. I dont feel much difference but because I'm not working (just started 4 weeks off sick) I do feel marginally more capable of day to day activities. I'm also not as angry as I was last week.....☺️ But the tiredness is endless. I can have so much sleep and night
Hey everyone. I have my 5th shot due today. I dont feel much difference but because I'm not working (just started 4 weeks off sick) I do feel marginally more capable of day to day activities. I'm also not as angry as I was last week.....☺️ But the tiredness is endless. I can have so much sleep and night
Peppermints
in
Pernicious Anaemia Society
2 years ago
Autoimmune gastritis Vs AMAG/PA
https://pernicious-anaemia-society.org/b12deficiencyandperniciousanaemia/ This first article describes one cause of B12 deficiency (other than PA) as gastritis that is 'where the patient produces antibodies that destroy either the Parietal Cells or Intrinsic Factor or both.' So is this very much different
https://pernicious-anaemia-society.org/b12deficiencyandperniciousanaemia/ This first article describes one cause of B12 deficiency (other than PA) as gastritis that is 'where the patient produces antibodies that destroy either the Parietal Cells or Intrinsic Factor or both.' So is this very much different
myownscientist
in
Pernicious Anaemia Society
2 years ago
Can Ketone Esters provide Ketones without a Ketone diet?
Back in 2013, Dr. Mary Newport gave a Ted talk on her re-discovery of MCT oil (she'd been aware of it for several years). In short, it greatly helped her husband with AZ. More recently, Ketone Esters are said to be even more potent than MCT oil. This video is from Dr Newport's talk. I've started looking
Back in 2013, Dr. Mary Newport gave a Ted talk on her re-discovery of MCT oil (she'd been aware of it for several years). In short, it greatly helped her husband with AZ. More recently, Ketone Esters are said to be even more potent than MCT oil. This video is from Dr Newport's talk. I've started looking
JAS9
in
Cure Parkinson's
2 years ago
6 Red Flags to Watch Out For When Buying Vitamins & Supplements. As per Consumer Lab
I LUV consumer Lab "At ConsumerLab.com, we've purchased, tested, and carefully reviewed the labels of more than 6,000 dietary supplements and found problems with more than 20% of them." 1. Labels that don't tell you how much you're getting There are several situations where this can happen: "Proprietary
I LUV consumer Lab "At ConsumerLab.com, we've purchased, tested, and carefully reviewed the labels of more than 6,000 dietary supplements and found problems with more than 20% of them." 1. Labels that don't tell you how much you're getting There are several situations where this can happen: "Proprietary
MBAnderson
in
Cure Parkinson's
2 years ago
6 week dietary detox. Anyone want to join me? My goal is to have as optimum a diet as possible as part of my personal wellness program.
Tomorrow I am starting what I call my Optimum Self Care Dietary Detox. The impetus is to slow (hopefully stop) PD but I prefer to tell myself it is for “optimum wellness.” (If you want to tell me I’m delusional for thinking my diet can stop PD, please consider it as a coping skill. my self talk
Tomorrow I am starting what I call my Optimum Self Care Dietary Detox. The impetus is to slow (hopefully stop) PD but I prefer to tell myself it is for “optimum wellness.” (If you want to tell me I’m delusional for thinking my diet can stop PD, please consider it as a coping skill. my self talk
Hidden
in
Cure Parkinson's
2 years ago
Supplement, Iodine advice and more
Hi everyone Just need a little advice please. I am just not feeling right with headaches in morning, fuzzy head, fatigue and tummy upsets. I am trying to get to the bottom of why I am feeling so low. I came off thyroxine pills last May as I could not tolerate the fillers. After some hassle my GP
Hi everyone Just need a little advice please. I am just not feeling right with headaches in morning, fuzzy head, fatigue and tummy upsets. I am trying to get to the bottom of why I am feeling so low. I came off thyroxine pills last May as I could not tolerate the fillers. After some hassle my GP
Tintin0202
in
Thyroid UK
2 years ago
Newly diagnosed possible Autoimmune gastritis and B12 deficiency
I've recently started B12 injections under the care of a private doctor. He gave my first injection and I'm doing self injections at home (1mg hydroxocobalamin). My B12 was at 292 so a little above the NHS range but clearly deficient. I initially saw him to arrange an iron infusion for iron deficiency
I've recently started B12 injections under the care of a private doctor. He gave my first injection and I'm doing self injections at home (1mg hydroxocobalamin). My B12 was at 292 so a little above the NHS range but clearly deficient. I initially saw him to arrange an iron infusion for iron deficiency
myownscientist
in
Pernicious Anaemia Society
2 years ago
Confused, again
So had bloods repeated on NHS. All except 4 came back, on my GP no reference ranges. Got print outs and have been checking every day for missing results. Just now found 2 more on my GP. , had been waiting on T3 vit D and IFA and TTG (coeliac). One says intrinsic factor ab screen test but no
So had bloods repeated on NHS. All except 4 came back, on my GP no reference ranges. Got print outs and have been checking every day for missing results. Just now found 2 more on my GP. , had been waiting on T3 vit D and IFA and TTG (coeliac). One says intrinsic factor ab screen test but no
Polo22
in
Pernicious Anaemia Society
2 years ago
Any Advice on PA & B12 plus iron & ferritin
Hi I have Hypothyroidism and they have advised me to ask for your help . I will try & cut a long story short!! . Since 2018 I have had low Ferritin results quite often and have taken Ferrous fummerate for 6 months each time and then promptly ignored as problem solved . In December I had a blood test
Hi I have Hypothyroidism and they have advised me to ask for your help . I will try & cut a long story short!! . Since 2018 I have had low Ferritin results quite often and have taken Ferrous fummerate for 6 months each time and then promptly ignored as problem solved . In December I had a blood test
Spoticus
in
Pernicious Anaemia Society
2 years ago
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